5417-32-3 Usage
Description
1,3-DIOXEP-5-ENE, also known as 4,7-dihydro-1,3-dioxepin derivatives, is a chemical compound that undergoes hydroformylation to form optically active aldehydes. This process involves the conversion of an alkene to an aldehyde in the presence of a catalyst, typically a transition metal complex, and carbon monoxide and hydrogen.
Uses
Used in Pharmaceutical Industry:
1,3-DIOXEP-5-ENE is used as a key intermediate in the synthesis of various pharmaceutical compounds. The optically active aldehydes formed through hydroformylation can be further transformed into a wide range of biologically active molecules, making 1,3-DIOXEP-5-ENE a valuable building block in drug development.
Used in Chemical Synthesis:
1,3-DIOXEP-5-ENE is used as a versatile building block in organic synthesis for the creation of various chemical compounds. The optically active aldehydes derived from hydroformylation can be utilized in the synthesis of complex molecules, including chiral compounds, which are essential in various applications such as agrochemicals, fragrances, and specialty chemicals.
Used in Research and Development:
1,3-DIOXEP-5-ENE serves as an important compound in research and development, particularly in the field of asymmetric catalysis and enantioselective synthesis. The study of its hydroformylation process and the resulting optically active aldehydes can provide valuable insights into the development of new catalysts and synthetic methods, ultimately leading to more efficient and selective chemical transformations.
Check Digit Verification of cas no
The CAS Registry Mumber 5417-32-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,4,1 and 7 respectively; the second part has 2 digits, 3 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 5417-32:
(6*5)+(5*4)+(4*1)+(3*7)+(2*3)+(1*2)=83
83 % 10 = 3
So 5417-32-3 is a valid CAS Registry Number.
InChI:InChI=1/C5H8O2/c1-2-4-7-5-6-3-1/h1-2H,3-5H2
5417-32-3Relevant articles and documents
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Nouguier,R.,Gras,J-L.,Mchich,M.
, p. 2943 (1988)
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Process for the preparation of acetal copolymers with backbone bromo functional groups
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, (2008/06/13)
The invention concerns a method for producing an acetal copolymer containing backbone bromo-functional groups comprising copolymerizing trioxane with 5,6,-dibromo-1,3--dioxepene. The invention also concerns methods of modifying acetal copolymers containing bromo-functional groups and the copolymers produced by the methods of the invention.
Acetal copolymers with backbone double bonds
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, (2008/06/13)
Acetal copolymers of trioxane and 1,3-dioxep-5-ene having a high degree of crystallinity and specific mole percent incorporations of 1,3-dioxep-5-ene are synthesized. The invention also provides a process for producing highly crystalline acetal copolymers by copolymerizing trioxane and 1,3-dioxep-5-ene and precipitating the copolymer product from solution. The copolymers show much improved stability against halogen degradation.
